BEUDAMED
    2,193 results · 25ms · Sources: EU EUDAMED, US FDA

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    OC-Light S

    FDA UDI
    POLYMEDCO CANCER DIAGNOSTIC PRODUCTS LLC·00816917024578·Personal Use Kit OC-Light S, Custom Kit for Mel...

    Bausch + Lomb

    FDA UDI
    Bausch & Lomb Incorporated·00757770430475·SCS KERATO UTLY STICH CAST MIN

    Castroviejo Keratoplasty-Stitch Scissors

    FDA UDI
    Bausch & Lomb GmbH·04058935012151·

    ROCAWEAR

    FDA UDI
    Colors In Optics, Ltd.·00781268820943·Sunglasses

    ROCAWEAR

    FDA UDI
    Colors In Optics, Ltd.·00781268832533·Sunglasses

    MSI Precision Specialty Instruments

    FDA UDI
    Med Saver, Inc.·00194613008390·Castroviejo Mini Keratoplasty-Utility-Stitch Sc...

    CARDIOSAVE HYBRID TYPE B PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·November 20, 2020

    CARDIOSAVE HYBRID, TYPE B PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·April 17, 2025

    CARDIOSAVE HYBRID TYPE B PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·September 10, 2020

    CARDIOSAVE HYBRID, TYPE B PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·January 31, 2025

    CARDIOSAVE HYBRID, TYPE B PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·February 13, 2025

    CARDIOSAVE HYBRID TYPE B PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·August 31, 2021

    BD MAXPLUS¿ PRESSURE RATED EXTENSION SET WITH NEEDLELESS CONNECTOR AND Y-SITE

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·May 1, 2023

    DAVINCI XI

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·December 17, 2024

    CARDIOSAVE HYBRID, TYPE B PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·May 6, 2026

    MEDTRONIC ENRHYTHM

    FDA Adverse Event
    Injury ·MEDTRONIC·Product code NVZ·June 24, 2011

    CARDIOSAVE HYBRID, TYPE B PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·April 13, 2022

    ASR UNI FEMORAL IMPL SIZE 45

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD - 8010379·Product code KWA·November 21, 2021

    UNK HIP FEMORAL SLEEVE ASR

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD - 8010379·Product code KWA·November 21, 2021

    UNKNOWN HIP FEMORAL STEM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·November 21, 2021